Regulatory Submissions Jobs in Spain

Introduction to role:Are you ready to lead country-level clinical study delivery that accelerates breakthrough medicines to patients As Local Study Associate Director you will turn complex operational challenges into precise execution that safeguards data quality drives recruitment and keeps studies...

IQVIA Biotech is hiring Clinical Research Associate in Spain!IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure collaborative culture and deep therapeutic expertise allow us to deli...

Your missionWe are scientists doctors techies and humanity lovers with the mission of pioneering real time precision neurology to cure brain-related disorders. INBRAIN harnesses the extraordinary material properties of Graphene the worlds thinnest and nobel-prize winning material to build high resol...

Your missionWe are scientists doctors techies and humanity lovers with the mission of pioneering real time precision neurology to cure brain-related disorders. INBRAIN harnesses the extraordinary material properties of Graphene the worlds thinnest and nobel-prize winning material to build high resol...

Location:Barcelona - Spain (3 days working from the office and 2 days working from home)Introduction:The Director Principal Patient Safety Scientist role provides expertise to multiple and/or single but complex products in different stages of development as needed. He/she provides oversight of safet...

AboutSwan is Europes embedded banking specialist. We empower software companies to embed banking features like accounts cards and payments directly into their products under their own processes over 1.5 billion in monthly transactions for more than 150 companieslike Pennylane Indy Agicap Libeo and...

Regulatory Reporting FRA Analyst Own and execute daily / monthly production of FR 2052a FRY14 FRY15 liquidity reports ensuring completeness accuracy and timeliness. Prepare and validate FDIC regulatory reports in compliance with 12 CFR 369 (FDIC reporting requirements) and 12 CFR 370 (recordkeeping...

Site Activation Manager (Global)Sponsor FacingHomebasedJob OverviewLead and manage the strategic operational and financial delivery of Site Activation activities across assigned studies and regions. This role is responsible for accelerating site activation to support timely patient enrollment includ...

Galderma is the emerging pure-play dermatology category leader present in approximately 90 countries. We deliver an innovative science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics Dermatologic...

The Regulatory Expert Ecotoxicology acquires knowledge of recent regulatory scientific advances in the area of Ecotoxicology and is able to translate these into ways to organize and prepare registration dossiers for conventional and biological plant protection products. The Regulatory Expert Ecoto...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol applicable regulations and guidelines and sponsor requirements.Essential Functions Perform site monitoring visits (selection initiatio...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin us as a Senior Clinical Trial Manager - Make an Impact at the Forefront of InnovationThe Senior Clinical Trial Manager is accountable for achieving the final clinical deliverable (usually clean data from evaluable patie...

Galderma is the emerging pure-play dermatology category leader present in approximately 90 countries. We deliver an innovative science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics Dermatologic...

About This Role The Implantable Device Unit is looking to hire a Field Clinical Enginner (FCE) to support the clinical use and deployment of our Class III medical devices. The FCE will serve as a critical liaison between the company healthcare professionals and internal cross-functional teams. This...

About this roleTFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full-service capabilities resourcing and Functional Service (F...

Opportunity: Global Safety Program Lead - Cell Therapy Oncology & Onco-HematologyLocation:Barcelona Spain (on-site) 3 days working from the office and 2 days working from home.Do you haveexpertisein and passion for Patient Safety in Oncologyand Onco-Hematology Would you like to apply yourexpertiseto...

Opportunity: Global Safety Program Lead - Cell Therapy Oncology & Onco-HematologyLocation:Barcelona Spain (on-site) 3 days working from the office and 2 days working from home.Do you haveexpertisein and passion for Patient Safety in Oncologyand Onco-Hematology Would you like to apply yourexpertiseto...

Winid is a talent acquisition consultancy that offers Executive Search RPO and Talent Solutions.Our purpose is to drive the growth and fulfillment of individuals and organizations. We facilitate individuals in finding inspiring opportunities and help organizations discover professionals who will tak...

Location:Barcelona - Spain (3 days working from the office and 2 days working from home)Introduction to the roleThe Director Principal Patient Safety Scientist role provides expertise to multiple and/or single but complex products in different stages of development as needed. He/she provides oversig...